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甲状腺自身抗体在非人类大型猿类中罕见,而甲状腺功能减退症不能归因于甲状腺自身免疫。

Thyroid autoantibodies are rare in nonhuman great apes and hypothyroidism cannot be attributed to thyroid autoimmunity.

机构信息

Cedars-Sinai Medical Center, 8700 Beverly Boulevard, Suite B-131, Los Angeles, CA 90048.

出版信息

Endocrinology. 2013 Dec;154(12):4896-907. doi: 10.1210/en.2013-1717. Epub 2013 Oct 3.

Abstract

The great apes include, in addition to Homo, the genera Pongo (orangutans), Gorilla (gorillas), and Pan, the latter comprising two species, P. troglodytes (chimpanzees) and P. paniscus (bonobos). Adult-onset hypothyroidism was previously reported in 4 individual nonhuman great apes. However, there is scarce information on normal serum thyroid hormone levels and virtually no data for thyroid autoantibodies in these animals. Therefore, we examined thyroid hormone levels and TSH in all nonhuman great ape genera including adults, adolescents, and infants. Because hypothyroidism in humans is commonly the end result of thyroid autoimmunity, we also tested healthy and hypothyroid nonhuman great apes for antibodies to thyroglobulin (Tg), thyroid peroxidase (TPO), and the TSH receptor (TSHR). We established a thyroid hormone and TSH database in orangutans, gorillas, chimpanzees, and bonobos (447 individuals). The most striking differences are the greatly reduced free-T4 and free-T3 levels in orangutans and gorillas vs chimpanzees and bonobos, and conversely, elevated TSH levels in gorillas vs Pan species. Antibodies to Tg and TPO were detected in only 2.6% of adult animals vs approximately 10% in humans. No animals with Tg, TPO, or TSHR antibodies exhibited thyroid dysfunction. Conversely, hypothyroid nonhuman great apes lacked thyroid autoantibodies. Moreover, thyroid histology in necropsy tissues was similar in euthyroid and hypothyroid individuals, and lymphocytic infiltration was absent in 2 hypothyroid animals. In conclusion, free T4 and free T3 are lower in orangutans and gorillas vs chimpanzees and bonobos, the closest living human relatives. Moreover, thyroid autoantibodies are rare and hypothyroidism is unrelated to thyroid autoimmunity in nonhuman great apes.

摘要

大型猿类除了人类(Homo)外,还包括猩猩属(Pongo,猩猩)、大猩猩属(Gorilla,大猩猩)和人属(Pan),后者包括两个物种,即黑猩猩(P. troglodytes)和倭黑猩猩(P. paniscus)。以前曾有报道称,4 只非人类大型猿类患有成人发病型甲状腺功能减退症。然而,关于这些动物的正常血清甲状腺激素水平的信息很少,几乎没有关于甲状腺自身抗体的数据。因此,我们检查了包括成年、青少年和婴儿在内的所有非人类大型猿类的甲状腺激素水平和 TSH。由于人类的甲状腺功能减退症通常是甲状腺自身免疫的结果,我们还测试了健康和患有甲状腺功能减退症的非人类大型猿类的甲状腺球蛋白(Tg)、甲状腺过氧化物酶(TPO)和 TSH 受体(TSHR)抗体。我们在猩猩、大猩猩、黑猩猩和倭黑猩猩中建立了一个甲状腺激素和 TSH 数据库(447 个人)。最显著的差异是猩猩和大猩猩的游离-T4 和游离-T3 水平大大降低,而黑猩猩和倭黑猩猩的水平较高,相反,大猩猩的 TSH 水平高于 Pan 物种。只有 2.6%的成年动物检测到 Tg 和 TPO 抗体,而人类中约有 10%。没有 Tg、TPO 或 TSHR 抗体的动物表现出甲状腺功能障碍。相反,患有甲状腺功能减退症的非人类大型猿类缺乏甲状腺自身抗体。此外,尸检组织中的甲状腺组织学在甲状腺功能正常和甲状腺功能减退的个体中相似,并且在 2 只甲状腺功能减退的动物中不存在淋巴细胞浸润。总之,与黑猩猩和倭黑猩猩相比,猩猩和大猩猩的游离 T4 和游离 T3 水平较低,黑猩猩和倭黑猩猩是与人类关系最近的活体动物。此外,非人类大型猿类的甲状腺自身抗体罕见,甲状腺功能减退症与甲状腺自身免疫无关。

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